Development of a clinical trial to determine whether watchful waiting is an acceptable alternative to surgical repair for patients with oligosymptomatic incisional hernia: study protocol for a randomized controlled trial

<p>Abstract</p> <p>Background</p> <p>Incisional hernia is a frequent complication in abdominal surgery. This article describes the development of a prospective randomized clinical trial designed to determine whether watchful waiting is an acceptable alternative to surgi...

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Main Authors: Lauscher Johannes C, Martus Peter, Stroux Andrea, Neudecker Jens, Behrens Uwe, Hammerich Ralf, Buhr Heinz J, Ritz Jörg-Peter
Format: Article
Language:English
Published: BMC 2012-02-01
Series:Trials
Subjects:
Online Access:http://www.trialsjournal.com/content/13/1/14
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spelling doaj-2aa45511414c4b4293472534d3f49a992020-11-24T23:28:20ZengBMCTrials1745-62152012-02-011311410.1186/1745-6215-13-14Development of a clinical trial to determine whether watchful waiting is an acceptable alternative to surgical repair for patients with oligosymptomatic incisional hernia: study protocol for a randomized controlled trialLauscher Johannes CMartus PeterStroux AndreaNeudecker JensBehrens UweHammerich RalfBuhr Heinz JRitz Jörg-Peter<p>Abstract</p> <p>Background</p> <p>Incisional hernia is a frequent complication in abdominal surgery. This article describes the development of a prospective randomized clinical trial designed to determine whether watchful waiting is an acceptable alternative to surgical repair for patients with oligosymptomatic incisional hernia.</p> <p>Methods/Design</p> <p>This clinical multicenter trial has been designed to compare watchful waiting and surgical repair for patients with oligosymptomatic incisional hernia. Participants are randomized to watchful waiting or surgery and followed up for two years. The primary efficacy endpoint is pain/discomfort during normal activities as a result of the hernia or hernia repair two years after enrolment, as measured by the hernia-specific Surgical Pain Scales (SPS). The target sample size of six hundred thirty-six patients was calculated to detect non-inferiority of the experimental intervention (watchful waiting) in the primary endpoint. Sixteen surgical centers will take part in the study and have submitted their declaration of commitment giving the estimated number of participating patients per year. A three-person data safety monitoring board will meet annually to monitor and supervise the trial.</p> <p>Discussion</p> <p>To date, we could find no published data on the natural course of incisional hernias. To our knowledge, watchful waiting has never been compared to standard surgical repair as a treatment option for incisional hernias. A trial to compare the outcome of the two approaches in patients with oligosymptomatic incisional hernias is urgently needed to provide data that can facilitate the choice between treatment options. If watchful waiting was equal to surgical repair, the high costs of surgical repair could be saved. The design for such a trial is described here.</p> <p>This multicenter trial will be funded by the German Research Foundation (DFG). The ethics committee of the Charité has approved the study protocol. Approval has been obtained from ten study sites at time of this submission. The electronic Case Report Forms have been created. The first patient was to be randomized November 14<sup>th</sup>, 2011. An initiation meeting took place in Berlin January 9<sup>th</sup>, 2012.</p> <p>Trial Registration</p> <p>ClinicalTrials.gov: <a href="http://www.clinicaltrials.gov/ct2/show/NCT01349400">NCT01349400</a></p> http://www.trialsjournal.com/content/13/1/14oligosymptomatic incisional herniawatchful waitingsurgical repairprospective randomized trial
collection DOAJ
language English
format Article
sources DOAJ
author Lauscher Johannes C
Martus Peter
Stroux Andrea
Neudecker Jens
Behrens Uwe
Hammerich Ralf
Buhr Heinz J
Ritz Jörg-Peter
spellingShingle Lauscher Johannes C
Martus Peter
Stroux Andrea
Neudecker Jens
Behrens Uwe
Hammerich Ralf
Buhr Heinz J
Ritz Jörg-Peter
Development of a clinical trial to determine whether watchful waiting is an acceptable alternative to surgical repair for patients with oligosymptomatic incisional hernia: study protocol for a randomized controlled trial
Trials
oligosymptomatic incisional hernia
watchful waiting
surgical repair
prospective randomized trial
author_facet Lauscher Johannes C
Martus Peter
Stroux Andrea
Neudecker Jens
Behrens Uwe
Hammerich Ralf
Buhr Heinz J
Ritz Jörg-Peter
author_sort Lauscher Johannes C
title Development of a clinical trial to determine whether watchful waiting is an acceptable alternative to surgical repair for patients with oligosymptomatic incisional hernia: study protocol for a randomized controlled trial
title_short Development of a clinical trial to determine whether watchful waiting is an acceptable alternative to surgical repair for patients with oligosymptomatic incisional hernia: study protocol for a randomized controlled trial
title_full Development of a clinical trial to determine whether watchful waiting is an acceptable alternative to surgical repair for patients with oligosymptomatic incisional hernia: study protocol for a randomized controlled trial
title_fullStr Development of a clinical trial to determine whether watchful waiting is an acceptable alternative to surgical repair for patients with oligosymptomatic incisional hernia: study protocol for a randomized controlled trial
title_full_unstemmed Development of a clinical trial to determine whether watchful waiting is an acceptable alternative to surgical repair for patients with oligosymptomatic incisional hernia: study protocol for a randomized controlled trial
title_sort development of a clinical trial to determine whether watchful waiting is an acceptable alternative to surgical repair for patients with oligosymptomatic incisional hernia: study protocol for a randomized controlled trial
publisher BMC
series Trials
issn 1745-6215
publishDate 2012-02-01
description <p>Abstract</p> <p>Background</p> <p>Incisional hernia is a frequent complication in abdominal surgery. This article describes the development of a prospective randomized clinical trial designed to determine whether watchful waiting is an acceptable alternative to surgical repair for patients with oligosymptomatic incisional hernia.</p> <p>Methods/Design</p> <p>This clinical multicenter trial has been designed to compare watchful waiting and surgical repair for patients with oligosymptomatic incisional hernia. Participants are randomized to watchful waiting or surgery and followed up for two years. The primary efficacy endpoint is pain/discomfort during normal activities as a result of the hernia or hernia repair two years after enrolment, as measured by the hernia-specific Surgical Pain Scales (SPS). The target sample size of six hundred thirty-six patients was calculated to detect non-inferiority of the experimental intervention (watchful waiting) in the primary endpoint. Sixteen surgical centers will take part in the study and have submitted their declaration of commitment giving the estimated number of participating patients per year. A three-person data safety monitoring board will meet annually to monitor and supervise the trial.</p> <p>Discussion</p> <p>To date, we could find no published data on the natural course of incisional hernias. To our knowledge, watchful waiting has never been compared to standard surgical repair as a treatment option for incisional hernias. A trial to compare the outcome of the two approaches in patients with oligosymptomatic incisional hernias is urgently needed to provide data that can facilitate the choice between treatment options. If watchful waiting was equal to surgical repair, the high costs of surgical repair could be saved. The design for such a trial is described here.</p> <p>This multicenter trial will be funded by the German Research Foundation (DFG). The ethics committee of the Charité has approved the study protocol. Approval has been obtained from ten study sites at time of this submission. The electronic Case Report Forms have been created. The first patient was to be randomized November 14<sup>th</sup>, 2011. An initiation meeting took place in Berlin January 9<sup>th</sup>, 2012.</p> <p>Trial Registration</p> <p>ClinicalTrials.gov: <a href="http://www.clinicaltrials.gov/ct2/show/NCT01349400">NCT01349400</a></p>
topic oligosymptomatic incisional hernia
watchful waiting
surgical repair
prospective randomized trial
url http://www.trialsjournal.com/content/13/1/14
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